Remifentanil and Controlled Hypotension for Functional Endoscopic Sinus Surgery: Comparison With Tramadol and Metoprolol
Information source: Rize niversitesi
ClinicalTrials.gov processed this data on August 23, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Nasal Polyps
Intervention: Remifentanil (Drug); Tramadol (Drug); Metoprolol (Drug)
Phase: Phase 4
Status: Recruiting
Sponsored by: Rize niversitesi Official(s) and/or principal investigator(s): Başar Erdivanlı, Asst. Prof., Principal Investigator, Affiliation: Recep Tayyip Erdogan University, Medical Faculty, Department of Anesthesiology and Reanimation
Overall contact: Başar Erdivanlı, Asst. Prof., Phone: 04642130491, Ext: 2128, Email: basar.erdivanli@erdogan.edu.tr
Summary
Functional endoscopic sinus surgery (FESS) is indicated in diseases such as chronic
sinusitis refractory to medical treatment, nasal polyposis, mass lesions in the nasal
cavity. The purpose of this study is to determine whether tramadol and metoprolol are as
effective as remifentanil in providing controlled hypotension during FESS.
Clinical Details
Official title: Remifentanil and Controlled Hypotension for Functional Endoscopic Sinus Surgery: Comparison With Tramadol and Metoprolol
Study design: Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor)
Primary outcome: Composite outcome measure: variation of intraoperative blood pressure
Secondary outcome: Composite outcome measure: variation of intraoperative heart rateIntraoperative bleeding score Postoperative pain scores
Detailed description:
This study aims to compare two techniques for controlled hypotension during FESS. In both
cases, the patients will be evaluated during the preoperative anesthetic visit, and will be
given care by an anesthesiologist during the perioperative period.
Patients who are scheduled for an elective FESS operation will be included in the study.
During the preoperative anaesthetic visit, patients who do not meet any of the the exclusion
criteria will be offered to participate in hte study. Patients accepting to contribute tot
he study will be randomised into one of the two groups via closed envelope technique.
A pilot study with 20 patients resulted in similar means and slightly different standard
deviations of mean blood pressure. This pilot study showed that 44 patients in each group
are sufficient to obtain 80% power with an alpha error of 0. 05 and beta error of 20%. To
compensate for missing/inconsistent data, or allow for better matching of the demographic
variables, 3-5 additional patients will be recruited.
The anesthesiologist in charge of the patient will not be blinded to the groups, and will be
responsible for maintaining the hypotension (and patient safety) with either remifentanil in
one group, or tramadol and metoprolol in the other group. Systolic, diastolic, and mean
blood pressures, and heart rate will be recorded into a spreadsheet every three minutes
during the anaesthetic and surgical period. The data will be recorded via an excel form,
which will validate the entries upon entrance. The accuracy and completeness of registry
data will be verified by a third investigator, who will compare the registry data to the
medical monitor records at the end of each operative day.
The surgeon will be blinded to the groups, and will be responsible for scoring the surgical
vision and bleeding with the intraoperative bleeding score. The study drugs will be
administered via the same type of infusion pump to facilitate the blinding process.
Any adverse event will be reported in the patient chart and study records.
Statistical analysis will be carried out using R and SPSS (Statistical Package for the
Social Sciences) programs. Demographic variables (age, gender, American Society of
Anesthesiologists (ASA) score, comorbidities) will be analysed using descriptive statistics.
Study variables such as duration of operation, variance of the hemodynamic parameters,
amount of bleeding, bleeding score, occurrence of adverse events will be analysed with the
appropriate statistical tests.
Eligibility
Minimum age: 20 Years.
Maximum age: 65 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- diagnosis of rhinosinusitis
- indication for functional endoscopic sinus surgery
Exclusion Criteria:
- American Society of Anesthesiologists risk score > 2
- undertreated hypertension
- HgA1C (hemoglobin A1c test) level > 7. 5
- pregnancy
- concurrent surgery
- history of drug abuse
- history of or new diagnosis of allergy to any of the study drugs
- history of post-operative nausea and vomiting
Locations and Contacts
Başar Erdivanlı, Asst. Prof., Phone: 04642130491, Ext: 2128, Email: basar.erdivanli@erdogan.edu.tr
Recep Tayyip Erdogan University, Rize, Eastern Blacksea 53100, Turkey; Recruiting Başar Erdivanlı, Asst, Phone: 04642130491, Ext: 2128, Email: basar.erdivanli@erdogan.edu.tr Özlem Çelebi Erdivanlı, Asst, Phone: 04642130491, Ext: 1392, Email: ozlem.celebi@erdogan.edu.tr
Additional Information
Related publications: Hosemann W, Draf C. Danger points, complications and medico-legal aspects in endoscopic sinus surgery. GMS Curr Top Otorhinolaryngol Head Neck Surg. 2013 Dec 13;12:Doc06. doi: 10.3205/cto000098. Review. Cinčikas D, Ivaškevičius J, Martinkėnas JL, Balseris S. A role of anesthesiologist in reducing surgical bleeding in endoscopic sinus surgery. Medicina (Kaunas). 2010;46(11):730-4. Review. Lin D, Dalgorf D, Witterick IJ. Predictors of unexpected hospital admissions after outpatient endoscopic sinus surgery: retrospective review. J Otolaryngol Head Neck Surg. 2008 Jun;37(3):309-11. Komatsu R, Turan AM, Orhan-Sungur M, McGuire J, Radke OC, Apfel CC. Remifentanil for general anaesthesia: a systematic review. Anaesthesia. 2007 Dec;62(12):1266-80. Review. Rathjen T, Bockmühl U, Greim CA. [Modern anesthesiologic concepts supporting paranasal sinus surgery]. Laryngorhinootologie. 2006 Jan;85(1):20-3. German. Khalil HS, Nunez DA. Functional endoscopic sinus surgery for chronic rhinosinusitis. Cochrane Database Syst Rev. 2006 Jul 19;(3):CD004458. Review. Sartcaoglu F, Celiker V, Basgul E, Yapakci O, Aypar U. The effect of hypotensive anaesthesia on cognitive functions and recovery at endoscopic sinus surgery. Eur J Anaesthesiol. 2005 Feb;22(2):157-9.
Starting date: January 2015
Last updated: June 25, 2015
|